Canonical Allele Identifier: CA559281851
Gene: PLCXD3 HGNC NCBI

Linked Data

dbSNP Id: rs1208408587
gnomAD v2: 5-41475778-G-A
gnomAD v4: 5-41475676-G-A
MyVariant Identifiers: chr5:g.41475778G>A (hg19) chr5:g.41475676G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.41475676G>A , CM000667.2:g.41475676G>A GRCh38
NC_000005.9:g.41475778G>A , CM000667.1:g.41475778G>A GRCh37
NC_000005.8:g.41511535G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377801.8:c.103+34748C>T MANE Select ENSP00000367032.3:n.103+34748C>T
ENST00000328457.5:c.103+34748C>T ENSP00000333751.3:n.103+34748C>T
ENST00000377801.7:c.103+34748C>T ENSP00000367032.3:n.103+34748C>T
NM_001005473.2:c.103+34748C>T NP_001005473.1:n.103+34748C>T
NM_001005473.3:c.103+34748C>T MANE Select NP_001005473.1:n.103+34748C>T
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